Study Results
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Basic Information
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COMPLETED
60 participants
OBSERVATIONAL
2013-12-31
2014-11-30
Brief Summary
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Detailed Description
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According to study design, subjects were divided into three groups based on their periodontal parameters. Patients suffering from chronic periodontitis formed the group 1 (n: 20), patients with plaque induced gingivitis formed the group 2 (n:20) and periodontal healthy patients were inserted in group 3 (n:20).
After gently drying the area, GCF was sampled with filter paper using the intracrevicular method (Periopaper, ProFlow, Inc., Amityville, New York, USA).Two milliliters (ml) of peripheral blood was collected from each individual with sterile syringe from the antecubital fossa by venipuncture, and to separate serum component sample centrifuged at 3000g for 5 min, and immediately stored at -40°C until assayed.
The quantity of Fetuin-A and SAA protein concentration in the samples were analyzed by sandwich enzyme-linked immunosorbent assay (ELISA) procedures using commercially available kits.
The Spearman's rank correlation test was used to detect the relationship between GCF and serum SAA and Fetuin-A with GI and CAL. All tests were performed using statistical software (SPSS Inc., version 22.0, Chicago, IL, USA). The mean ± standard deviation with mean rank values were calculated for each parameter, based on the patients as the statistical unit. P \< 0.05 was considered to be statistically significant.
Conditions
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Study Design
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CASE_CONTROL
CROSS_SECTIONAL
Study Groups
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Group 1
Chronic Periodontitis-serum amyloid A, Fetuin-A
Fetuin-A
Acute phase protein
Serum Amyloid A
Acute phase protein
Group 2
Plaque induced Gingivitis-serum amyloid A, Fetuin-A
Fetuin-A
Acute phase protein
Serum Amyloid A
Acute phase protein
Group 3
Control Group-serum amyloid A, Fetuin-A
Fetuin-A
Acute phase protein
Serum Amyloid A
Acute phase protein
Interventions
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Fetuin-A
Acute phase protein
Serum Amyloid A
Acute phase protein
Eligibility Criteria
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Inclusion Criteria
* Systematically healthy patients
* No alveolar bone and attachment loss
* Inflammation signs such as redness, edema and increased BOP levels,
* GI≥2, PPD≤3mm, CAL≤3mm.
* Systematically healthy patients
* No bone and attachment loss,
* GI=0, PPD≤3mm, CAL≤3mm
* Systematically healthy patients
Exclusion Criteria
* Oral pathologies,
* Patients with any other systemic diseases,
* Pregnant women and those in the lactation period,
* Patients with smoking habit and taking medication
* Patients received periodontal therapy in last 6 months
28 Years
45 Years
ALL
Yes
Sponsors
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Bulent Ecevit University
OTHER
Responsible Party
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ÇİĞDEM COŞKUN TÜRER
Dr.
Principal Investigators
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ÇİĞDEM COŞKUN TÜRER, PhD
Role: PRINCIPAL_INVESTIGATOR
BULENT ECEVIT UNIVERSITY FACULTY OF DENTISTRY DEPARTMENT OF PERIODONTOLOGY
Other Identifiers
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SAAFA1
Identifier Type: -
Identifier Source: org_study_id
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